| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
| rs6680396 | 1.000 | 0.040 | 1 | 196663340 | intron variant | A/G | snv | 0.22 | 3 | ||
| rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 3 | |
| rs10737670 | 1.000 | 0.040 | 1 | 196388616 | intron variant | A/C;G | snv | 0.27 | 2 | ||
| rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 2 | ||
| rs10754187 | 1.000 | 0.040 | 1 | 196447122 | intron variant | A/G;T | snv | 2 | |||
| rs10801530 | 1.000 | 0.040 | 1 | 196392367 | intron variant | G/T | snv | 0.27 | 2 | ||
| rs10801531 | 1.000 | 0.040 | 1 | 196394414 | intron variant | G/A | snv | 0.27 | 2 | ||
| rs10801532 | 1.000 | 0.040 | 1 | 196395046 | intron variant | A/G;T | snv | 2 | |||
| rs10801537 | 1.000 | 0.040 | 1 | 196457711 | intron variant | A/G | snv | 0.33 | 2 | ||
| rs10801551 | 1.000 | 0.040 | 1 | 196610909 | upstream gene variant | G/A;C | snv | 2 | |||
| rs10801560 | 1.000 | 0.040 | 1 | 196745470 | intron variant | C/A | snv | 0.19 | 2 | ||
| rs10801561 | 1.000 | 0.040 | 1 | 196745540 | intron variant | T/A | snv | 0.19 | 2 | ||
| rs10922071 | 1.000 | 0.040 | 1 | 196464740 | intron variant | G/A | snv | 0.33 | 2 | ||
| rs10922106 | 0.925 | 0.080 | 1 | 196722334 | intron variant | A/G | snv | 0.43 | 2 | ||
| rs10922144 | 1.000 | 0.040 | 1 | 196854170 | intron variant | C/A;T | snv | 2 | |||
| rs10922146 | 1.000 | 0.040 | 1 | 196865506 | intron variant | C/T | snv | 0.19 | 2 | ||
| rs10922147 | 1.000 | 0.040 | 1 | 196908559 | intron variant | C/G | snv | 0.22 | 2 | ||
| rs11807331 | 1.000 | 0.040 | 1 | 196458681 | intron variant | T/C | snv | 0.33 | 2 | ||
| rs12029571 | 1.000 | 0.040 | 1 | 196634172 | intergenic variant | A/G | snv | 0.24 | 2 | ||
| rs12041668 | 1.000 | 0.040 | 1 | 196693917 | intron variant | C/T | snv | 0.19 | 2 | ||
| rs12047098 | 1.000 | 0.040 | 1 | 196865976 | intron variant | T/C | snv | 0.19 | 2 | ||
| rs12061508 | 1.000 | 0.040 | 1 | 196615338 | intergenic variant | G/A | snv | 0.23 | 2 | ||
| rs12065463 | 1.000 | 0.040 | 1 | 196495624 | intron variant | T/C | snv | 0.33 | 2 |